ATE405289T1 - 6-FLUOROBICYCLO 3.1.0 HEXANE DERIVATIVES - Google Patents

6-FLUOROBICYCLO 3.1.0 HEXANE DERIVATIVES

Info

Publication number
ATE405289T1
ATE405289T1 AT02793421T AT02793421T ATE405289T1 AT E405289 T1 ATE405289 T1 AT E405289T1 AT 02793421 T AT02793421 T AT 02793421T AT 02793421 T AT02793421 T AT 02793421T AT E405289 T1 ATE405289 T1 AT E405289T1
Authority
AT
Austria
Prior art keywords
group
alkoxy
represent
fluorobicyclo
different
Prior art date
Application number
AT02793421T
Other languages
German (de)
Inventor
Atsuro Nakazato
Shigeyuki Chaki
Kazunari Sakagami
Ryoko Dean
Hiroshi Ohta
Shiho Hirota
Akito Yasuhara
Original Assignee
Taisho Pharmaceutical Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Taisho Pharmaceutical Co Ltd filed Critical Taisho Pharmaceutical Co Ltd
Application granted granted Critical
Publication of ATE405289T1 publication Critical patent/ATE405289T1/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/196Carboxylic acids, e.g. valproic acid having an amino group the amino group being directly attached to a ring, e.g. anthranilic acid, mefenamic acid, diclofenac, chlorambucil
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/38Heterocyclic compounds having sulfur as a ring hetero atom
    • A61K31/381Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/185Acids; Anhydrides, halides or salts thereof, e.g. sulfur acids, imidic, hydrazonic or hydroximic acids
    • A61K31/19Carboxylic acids, e.g. valproic acid
    • A61K31/195Carboxylic acids, e.g. valproic acid having an amino group
    • A61K31/197Carboxylic acids, e.g. valproic acid having an amino group the amino and the carboxyl groups being attached to the same acyclic carbon chain, e.g. gamma-aminobutyric acid [GABA], beta-alanine, epsilon-aminocaproic acid, pantothenic acid
    • A61K31/198Alpha-aminoacids, e.g. alanine, edetic acids [EDTA]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/08Antiepileptics; Anticonvulsants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/14Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
    • A61P25/16Anti-Parkinson drugs
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/18Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/28Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/30Drugs for disorders of the nervous system for treating abuse or dependence
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/46Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton
    • C07C229/50Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino or carboxyl groups bound to carbon atoms of rings other than six-membered aromatic rings of the same carbon skeleton with amino groups and carboxyl groups bound to carbon atoms being part of the same condensed ring system
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/02Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton
    • C07C237/04Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atoms of the carboxamide groups bound to acyclic carbon atoms of the carbon skeleton the carbon skeleton being acyclic and saturated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/24Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring of the carbon skeleton
    • C07C237/26Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a ring other than a six-membered aromatic ring of the carbon skeleton of a ring being part of a condensed ring system formed by at least four rings, e.g. tetracycline
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/49Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/54Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and etherified hydroxy groups bound to the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/14Radicals substituted by singly bound hetero atoms other than halogen
    • C07D333/16Radicals substituted by singly bound hetero atoms other than halogen by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/06Systems containing only non-condensed rings with a five-membered ring
    • C07C2601/08Systems containing only non-condensed rings with a five-membered ring the ring being saturated
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2602/00Systems containing two condensed rings
    • C07C2602/02Systems containing two condensed rings the rings having only two atoms in common
    • C07C2602/14All rings being cycloaliphatic
    • C07C2602/18All rings being cycloaliphatic the ring system containing six carbon atoms

Abstract

An antidepressant comprising, as an active ingredient, a compound having an antagonistic effect on group II metabotropic glutamate receptors, as well as a 2-amino-3-alkoxy-6-fluoro-bicycloÄ3.1.0Ühexane-2,6-dicarboxylic acid derivative of Formula ÄIÜ: <CHEM> Äwherein R<1> and R<2>, which may be the same or different, each represent a hydroxyl group, a C1-10 alkoxy group, etc.; R<3> represents a C1-10 acyl group, a C1-6 alkoxy-C1-6 acyl group, etc.; and R<4> and R<5>, which may be the same or different, each represent a hydrogen atom, a C1-10 alkyl group, etc.Ü or a pharmaceutically acceptable salt or hydrate thereof.
AT02793421T 2001-12-27 2002-12-26 6-FLUOROBICYCLO 3.1.0 HEXANE DERIVATIVES ATE405289T1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001395797 2001-12-27

Publications (1)

Publication Number Publication Date
ATE405289T1 true ATE405289T1 (en) 2008-09-15

Family

ID=27602080

Family Applications (1)

Application Number Title Priority Date Filing Date
AT02793421T ATE405289T1 (en) 2001-12-27 2002-12-26 6-FLUOROBICYCLO 3.1.0 HEXANE DERIVATIVES

Country Status (24)

Country Link
US (1) US7157594B2 (en)
EP (1) EP1459765B1 (en)
JP (1) JP4230919B2 (en)
KR (2) KR100897970B1 (en)
CN (1) CN1281274C (en)
AT (1) ATE405289T1 (en)
AU (1) AU2002359923B2 (en)
BR (1) BR0215462A (en)
CA (1) CA2471642C (en)
CY (1) CY1108380T1 (en)
DE (1) DE60228491D1 (en)
DK (1) DK1459765T3 (en)
ES (1) ES2311642T3 (en)
HK (1) HK1073258A1 (en)
HU (1) HU228436B1 (en)
MX (1) MXPA04006322A (en)
NO (1) NO328844B1 (en)
NZ (1) NZ533699A (en)
PL (1) PL208123B1 (en)
PT (1) PT1459765E (en)
RU (1) RU2315622C2 (en)
SI (1) SI1459765T1 (en)
WO (1) WO2003061698A1 (en)
ZA (2) ZA200404795B (en)

Families Citing this family (47)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MXPA03003690A (en) * 2000-10-27 2004-05-05 Chiron Spa Nucleic acids and proteins from streptococcus groups a b.
PT1517915E (en) * 2002-06-11 2009-04-09 Lilly Co Eli Prodrugs of excitatory amino acids
US7109383B2 (en) * 2002-09-27 2006-09-19 Central Glass Company, Limited Fluorine-containing allyl ether compounds, their copolymers, and resist compositions and anti-reflection film materials using such copolymers
NZ580554A (en) 2003-06-26 2011-01-28 Taisho Pharmaceutical Co Ltd 2-Aminobicyclo[3.1.0]hexane-2,6-dicarboxylic ester derivative
JP5485492B2 (en) * 2004-12-15 2014-05-07 大正製薬株式会社 Drugs for the prevention and treatment of depression
EP2258359A3 (en) 2005-08-26 2011-04-06 Braincells, Inc. Neurogenesis by muscarinic receptor modulation with sabcomelin
JP2009506069A (en) 2005-08-26 2009-02-12 ブレインセルス,インコーポレイティド Neurogenesis through modulation of muscarinic receptors
AU2006304787A1 (en) 2005-10-21 2007-04-26 Braincells, Inc. Modulation of neurogenesis by PDE inhibition
CA2625210A1 (en) 2005-10-31 2007-05-10 Braincells, Inc. Gaba receptor mediated modulation of neurogenesis
US20100216734A1 (en) 2006-03-08 2010-08-26 Braincells, Inc. Modulation of neurogenesis by nootropic agents
AR059898A1 (en) 2006-03-15 2008-05-07 Janssen Pharmaceutica Nv DERIVATIVES OF 3-CIANO-PIRIDONA 1,4-DISUSTITUTED AND ITS USE AS ALLOSTERIC MODULATORS OF MGLUR2 RECEIVERS
EP2026813A2 (en) 2006-05-09 2009-02-25 Braincells, Inc. 5 ht receptor mediated neurogenesis
EP2377531A2 (en) 2006-05-09 2011-10-19 Braincells, Inc. Neurogenesis by modulating angiotensin
US7998971B2 (en) 2006-09-08 2011-08-16 Braincells Inc. Combinations containing a 4-acylaminopyridine derivative
US20100184806A1 (en) 2006-09-19 2010-07-22 Braincells, Inc. Modulation of neurogenesis by ppar agents
TW200900065A (en) 2007-03-07 2009-01-01 Janssen Pharmaceutica Nv 3-cyano-4-(4-pyridinyloxy-phenyl)-pyridin-2-one derivatives
TW200845978A (en) 2007-03-07 2008-12-01 Janssen Pharmaceutica Nv 3-cyano-4-(4-tetrahydropyran-phenyl)-pyridin-2-one derivatives
CN101801951B (en) 2007-09-14 2013-11-13 杨森制药有限公司 1',3'-disubstituted-4-phenyl-3,4,5,6-tetrahydro-2h, 1'h-[1, 4'] bipyridinyl-2'-ones
KR20100065191A (en) 2007-09-14 2010-06-15 오르토-맥닐-얀센 파마슈티칼스 인코포레이티드 1,3-disubstituted 4-(aryl-x-phenyl)-1h-pyridin-2-ones
TW200927731A (en) 2007-09-14 2009-07-01 Ortho Mcneil Janssen Pharm 1,3-disubstituted-4-phenyl-1H-pyridin-2-ones
ES2637794T3 (en) 2007-11-14 2017-10-17 Janssen Pharmaceuticals, Inc. Imidazo [1,2-A] pyridine derivatives and their use as positive allosteric modulators of MGLUR2 receptors
RU2510396C2 (en) 2008-09-02 2014-03-27 Янссен Фармасьютикалз, Инк. 3-azabicyclo[3,1,0]hexyl derivatives as modulators of metabotropic glutamate receptors
BRPI0920354A2 (en) 2008-10-16 2017-06-27 Addex Pharmaceuticals Sa indole and benzomorpholine derivatives as metabotropic glutamate receptor modulators
AU2009319387B2 (en) 2008-11-28 2012-05-10 Addex Pharma S.A. Indole and benzoxazine derivatives as modulators of metabotropic glutamate receptors
US20100216805A1 (en) 2009-02-25 2010-08-26 Braincells, Inc. Modulation of neurogenesis using d-cycloserine combinations
RS53075B (en) 2009-05-12 2014-04-30 Janssen Pharmaceuticals Inc. 1,2,4-triazolo[4,3-a]pyridine derivatives and their use for the treatment or prevention of neurological and psychiatric disorders
MY153913A (en) 2009-05-12 2015-04-15 Janssen Pharmaceuticals Inc 7-aryl-1,2,4-triazolo[4,3-a]pyridine derivatives and their use as positive allosteric modulators of mglur2 receptors
JP5707390B2 (en) 2009-05-12 2015-04-30 ジャンセン ファーマシューティカルズ, インコーポレイテッド 1,2,4-Triazolo [4,3-a] pyridine derivatives and their use as positive allosteric modulators of the mGluR2 receptor
EP2502897B1 (en) 2009-11-18 2014-07-09 Taisho Pharmaceutical Co., Ltd. Method for producing optically active bicyclo [3.1.0]hexane derivative using enzyme
TW201124372A (en) 2009-11-19 2011-07-16 Taisho Pharmaceutical Co Ltd Process for producing 3-alkoxy-2-amino-6-fluorobicyclo[310]hexane-2,6-dicarboxylic acid derivative and intermediate thereof
EP2661435B1 (en) 2010-11-08 2015-08-19 Janssen Pharmaceuticals, Inc. 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS
EP2649069B1 (en) 2010-11-08 2015-08-26 Janssen Pharmaceuticals, Inc. 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS
EP2643320B1 (en) 2010-11-08 2015-03-04 Janssen Pharmaceuticals, Inc. 1,2,4-TRIAZOLO[4,3-a]PYRIDINE DERIVATIVES AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS
AR083845A1 (en) 2010-11-18 2013-03-27 Lilly Co Eli 3-PHENYLSULPHANYLME-BICYCLE COMPOUNDS [3.1.0] HEXANE 4-REPLACED AS ANTAGONISTS OF mGluR2 / 3
WO2012068041A1 (en) 2010-11-18 2012-05-24 Eli Lilly And Company 4-SUBSTITUTED-3-BENZYLOXY-BICYCLO[3.1.0]HEXANE COMPOUNDS AS mGluR 2/3 ANTAGONISTS
PT2721012T (en) 2011-06-17 2016-07-27 Lilly Co Eli Bicyclo(3.1.0)hexane-2,6-dicarboxylic acid derivatives as mglu2 receptor agonist
WO2013062680A1 (en) * 2011-10-25 2013-05-02 Braincells, Inc. Novel compounds and compositions thereof for treating nervous system disorders
RU2496495C2 (en) * 2011-12-05 2013-10-27 Учреждение Российской академии медицинских наук Научно-исследовательский институт нормальной физиологии имени П.К. Анохина РАМН USING SELECTIVE ANTAGONIST OF GLUAMATE RECEPTOR Ro-256981 FOR TARGETED EFFECT ON COGNITIVE FUNCTIONS
SG11201407973SA (en) * 2012-06-01 2015-01-29 Taisho Pharmaceutical Co Ltd Prodrug of fluorine-containing amino acid
JO3368B1 (en) 2013-06-04 2019-03-13 Janssen Pharmaceutica Nv 6,7-DIHYDROPYRAZOLO[1,5-a]PYRAZIN-4(5H)-ONE COMPOUNDS AND THEIR USE AS NEGATIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS
JO3367B1 (en) 2013-09-06 2019-03-13 Janssen Pharmaceutica Nv 1,2,4-TRIAZOLO[4,3-a]PYRIDINE COMPOUNDS AND THEIR USE AS POSITIVE ALLOSTERIC MODULATORS OF MGLUR2 RECEPTORS
DK3431106T3 (en) 2014-01-21 2021-03-15 Janssen Pharmaceutica Nv COMBINATIONS INCLUDING POSITIVE ALLOSTERIC MODULATORS OR ORTHOSTERIC AGONISTS OF METABOTROP GLUTAMATERG SUBTYPE 2 RECEPTOR AND USE OF THESE
ES2860298T3 (en) 2014-01-21 2021-10-04 Janssen Pharmaceutica Nv Combinations comprising positive allosteric modulators of metabotropic glutamatergic receptor subtype 2 and their use
DK3445743T3 (en) 2016-04-18 2021-10-18 Taisho Pharmaceutical Co Ltd PRODUCT OF AMINO ACID DERIVATIVE
JP7314494B2 (en) * 2017-10-17 2023-07-26 大正製薬株式会社 Pharmaceuticals containing prodrugs of amino acid derivatives
KR20220062838A (en) 2020-11-09 2022-05-17 대우조선해양 주식회사 Full spade rudder and ship having the same
JP2024004505A (en) * 2020-11-26 2024-01-17 大正製薬株式会社 Method for producing amino acid derivative

Family Cites Families (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA000894B1 (en) 1995-11-16 2000-06-26 Эли Лилли Энд Компани substituted bicyclohexanecarboxylic acids and derivatives thereof as excitatory amino acid receptor antagonists, method for producing and use thereof
ZA969485B (en) * 1995-11-16 1998-05-12 Lilly Co Eli Excitatory amino acid receptor antagonists.
ZA983930B (en) * 1997-05-14 1999-11-08 Lilly Co Eli Excitatory amino acid receptor modulators.
ATE269293T1 (en) 1998-08-31 2004-07-15 Taisho Pharmaceutical Co Ltd 6-FLUORO(3.1.0)HEXANE DERIVATIVES
JP4194715B2 (en) 1998-08-31 2008-12-10 大正製薬株式会社 6-Fluorobicyclo [3.1.0] hexane derivative
CH694053A5 (en) 1998-09-03 2004-06-30 Hoffmann La Roche Ver method for the production of 2-amino-bicyclo [3.1.0] hexane-2,6-dicarboxylic acid derivatives.
MXPA02000242A (en) 1999-06-30 2004-09-10 Prescient Neuropharma Inc 2-aminoindane analogs.
ATE265419T1 (en) * 2000-05-11 2004-05-15 Kenneth Curry SPIRO(2.4)HEPTANAMINOCARBOXIC ACID AND THEREOF DERIVATIVES
CA2411059A1 (en) 2000-06-28 2002-12-06 Taisho Pharmaceutical Co., Ltd. Novel dicarboxylic acid derivatives
NZ528315A (en) * 2001-04-12 2005-04-29 F Dihydro-benzo [b] [1, 4] diazepin-2-one derivatives as MGLUR2 antagonists II

Also Published As

Publication number Publication date
WO2003061698A1 (en) 2003-07-31
KR20090031962A (en) 2009-03-30
EP1459765B1 (en) 2008-08-20
ES2311642T3 (en) 2009-02-16
NZ533699A (en) 2006-05-26
NO20042530D0 (en) 2004-06-16
MXPA04006322A (en) 2004-10-04
HUP0402649A2 (en) 2005-10-28
KR100897970B1 (en) 2009-05-18
RU2004122916A (en) 2005-03-27
CN1610557A (en) 2005-04-27
CN1281274C (en) 2006-10-25
ZA200404795B (en) 2005-08-31
CA2471642A1 (en) 2003-07-31
EP1459765A1 (en) 2004-09-22
US7157594B2 (en) 2007-01-02
JP4230919B2 (en) 2009-02-25
BR0215462A (en) 2004-11-30
ZA200502085B (en) 2005-08-31
JPWO2003061698A1 (en) 2005-05-19
KR20040068348A (en) 2004-07-30
CY1108380T1 (en) 2014-02-12
HK1073258A1 (en) 2005-09-30
PL208123B1 (en) 2011-03-31
NO328844B1 (en) 2010-05-25
SI1459765T1 (en) 2009-02-28
RU2315622C2 (en) 2008-01-27
HU228436B1 (en) 2013-03-28
CA2471642C (en) 2011-05-24
US20050119345A1 (en) 2005-06-02
DK1459765T3 (en) 2008-10-06
AU2002359923B2 (en) 2007-12-20
EP1459765A4 (en) 2006-05-31
DE60228491D1 (en) 2008-10-02
PT1459765E (en) 2008-10-03
PL371014A1 (en) 2005-06-13
NO20042530L (en) 2004-09-22

Similar Documents

Publication Publication Date Title
ATE405289T1 (en) 6-FLUOROBICYCLO 3.1.0 HEXANE DERIVATIVES
EP1553089A4 (en) Antagonist of melanin-concentrating hormone receptor comprising benzimidazole derivative as active ingredient
DE69328856T2 (en) Hypoglycemic dihydrochalcone derivatives
ATE223378T1 (en) PROLINEAMIDE DERIVATIVES
WO2002010154A3 (en) Substituted heterocyclic amides
AU2003246100A1 (en) Amide derivative
HK1076816A1 (en)
NO20061832L (en) Carbamide derivatives of amide type
DK1043310T3 (en) Biphenylamidine derivatives
WO2003035610A1 (en) Sulfonamide derivative having mmp inhibitory activity
DE60104697D1 (en) SULFONAMIDE DERIVATIVES
ATE374750T1 (en) SEROTONIN RUPUP INHIBITORS
DK0978506T3 (en) 2-phenoxyaniline
NO20070421L (en) Radiosensitizing agent
ATE286878T1 (en) 3,4-DIHYDRO-1H-NAPHTHALINE DERIVATIVES AS HIGHLY SELECTIVE CYCLOOXYGENASE-2 INHIBITORS
DE60001205D1 (en) Azole derivatives or their salts
TR28240A (en) Insecticide, nematocide and acaricide containing amidothiophosphate derivative and active inhibitor.

Legal Events

Date Code Title Description
UEP Publication of translation of european patent specification

Ref document number: 1459765

Country of ref document: EP